recall
Akorn PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles)
Akorn recalls one lot of PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles) due to defective containers.
recall
Alaris infusion pumps
Becton Dickinson (BD)/Carefusion 303 recalls Alaris infusion pumps due to compatibility issues with Cardinal Health Monoject syringes. Use of…
recall
All ranitidine products (Zantac)
FDA requests removal of all ranitidine products (Zantac) from the market due to contamination with N-Nitrosodimethylamine (NDMA).
recall
Altaire Pharmaceuticals, Inc. recalls Perrigo brand ophthalmic products
Concerns about quality assurance controls
recall
American Health Packaging Valsartan Tablets, USP, 160 mg
Presence of probable human carcinogen N-Nitrosodiethylamine
recall
Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP
Presence of probable human carcinogen N-nitrosodiethylamine
recall
Amlodipine and Valsartan Tablets, USP; Valsartan Tablets, USP; and Valsartan and Hydrochlorothiazide Tablets, USP
Presence of probable carcinogen N-nitrosodiethylamine
recall
Amlodipine/Valsartan Combination Tablets and Amlodipine/Valsartan/Hydrochlorothiazide Combination Tablets
Presence above specification limits of probable carcinogen N-nitroso-diethylamine
recall
Ark Naturals Brushless Toothpaste Value Packs
Ark Naturals Brushless Toothpaste Value Packs recalled due to the potential for mold at some point during the product’s shelf life.
recall
Arrow MAC Two-Lumen Central Venous Access Kits
Teleflex and their subsidiary Arrow International, LLC recall Arrow MAC Two-Lumen Central Venous Access Kits and Arrow Pressure Injectable Arrowg+ard…
recall
Atovaquone Oral Suspension
Bionpharma Inc. is voluntarily recalling (1) single Batch (2310083) of Atovaquone Oral Suspension, 750mg per mL to the consumer level as the product…
recall
Aurobindo Pharma mirtazapine tablets
Aurobindo Pharma USA, Inc. recalls mirtazapine tablets due to a label error on declared strength.
recall
Aurobindo Quinapril and Hydrochlorothiazide Tablets USP 20mg/12.5mg
Aurobindo Pharma USA, Inc. recalls two lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, due to presence of Nitrosamine Drug…
recall
Aurobindo Pharma/ScieGen Pharmaceuticals Irbesartan
Presence of probable carcinogen N-nitrosodiethylamine
recall
AurobindoPharma Amlodipine Valsartan Tablets USP and Valsartan Tablets, USP (Expanded Recall)
Due to presence of probable carcinogen N-nitrosodiethylamine
recall
AurobindoPharma Acetris Valsartan Tablets, USP
Due to presence of probable carcinogen N-nitrosodiethylamine
recall
AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial
Eugia US LLC recalls lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial due to a…
recall
IV bags containing fentanyl or oxytocin & various prefilled syringes
Nephron Sterile Compounding Center recalls 2.1 million doses of medicine and medical equipment due to a lack of assurance of sterility.
recall
Banamine transdermal (flunixin transdermal solution)
Intervet, Inc banamine transdermal (flunixin transdermal solution) recalled due to leakage between the cap and bottle.
recall
Banamine® (flunixin meglumine injection)
Merck Animal Health recalls three batches of BANAMINE®/BANAMINE®-S (flunixin meglumine injection) 50 mg/mL due to the presence of particulate matter.
recall
Banamine® (flunixin meglumine injection) expanded recall
Merck Animal Health recalls four additional batches of BANAMINE®/BANAMINE®-S (flunixin meglumine injection) 50 mg/mL due to the presence of…
recall
Baxter Clearlink Basic Solution Set with Duovent
Baxter Healthcare recalls over half a million Clearlink Basic Solution Sets with Duovent (used for chemotherapy) due to a risk of leaks that may…
recall
Baxter DiscPac Syringe Tip Caps
Baxter recalls certain packages of DiscPac Syringe Tip Caps, Self-Righting, Luer Slip, because of the potential for the packaging to fail to maintain…
recall
Baxter Healthcare Corporation Novum IQ Syringe infusion system
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple…
